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Part Description

LP412148-1   Primary hyperoxaluria multigene analysis
Primary hyperoxaluria results from the overproduction of a substance called oxalate, which is excreted in the urine and can lead to stones in the form of calcium oxalate. This can lead to hematuria, urinary tract infections, kidney damage, end stage renal disease, as well as injury to other organs. There are 3 types 1,2 and 3 resulting from mutations in the AGXT, GRHPR, and HOGA1 genes respectively.[MedlinePlus Condition: primary-hyperoxaluria] Source: Regenstrief LOINC

LOINC Names Get Info

Fully-Specified Name
Primary hyperoxaluria multigene analysis:Find:Pt:Bld/Tiss:Doc:Molgen
Long Common Name
Primary hyperoxaluria multigene analysis in Blood or Tissue by Molecular genetics method
Short Name
PH Multigene Anl Bld/T
Display Name
Primary hyperoxaluria multigene analysis Molgen Doc (Bld/Tiss)
Consumer Name Alpha Get Info
Primary hyperoxaluria multigene analysis, Blood or tissue specimen

Part Model Get Info

  • Component
    Primary hyperoxaluria multigene analysis
    LP412148-1
    • Analyte
      Primary hyperoxaluria multigene analysis
      LP412148-1
      • Component Numerator
        Primary hyperoxaluria multigene analysis
        LP412148-1
        • Component Numerator Core
          Primary hyperoxaluria multigene analysis
          LP412148-1
        • Component Numerator Core Suffix
          NULL
           
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Find
    LP6813-2
  • Time
    Pt
    LP6960-1
  • System
    Bld/Tiss
    LP7061-7
    • System Core
      Bld/Tiss
      LP7061-7
    • Super System
      NULL
       
  • Scale
    Doc
    LP32888-7
  • Method
    Molgen
    LP6404-0

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.67
Last Updated
Version 2.67 (ADD)
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Primární hyperoxalurie multigenová analýza:Nález:Časový bod:Krev/tkáň:Dokument:Molekulární genetika
el-GRGreek (Greece)Πολυγονιδιακή ανάλυση πρωτοπαθούς υπεροξαλουρίας:Εύρεση:Pt:Αίμα/Ιστός:Doc:Μοριακή γενετική
Synonyms: Doc MOLPATH Pt Αίμα Αίμα/Ιστός Εύρεση Ιστός Μοριακή γενετική Πολυγονιδιακή ανάλυση πρωτοπαθούς υπεροξαλουρίας
es-ESSpanish (Spain)Análisis multigénico de hiperoxaluria primaria:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
es-MXSpanish (Mexico)Análisis multigénico de hiperoxaluria primaria:Hallazgo:Punto temporal:Sangre o tejido:Documento:Genética molecular
fr-FRFrench (France)Analyse multigénique d'une hyperoxalaturie primaire:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-ITItalian (Italy)Iperossaluria primaria, analisi multigenica:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Analisi multigenica dell''iperossaluria primaria Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
nl-NLDutch (Netherlands)multigen-analyse op primaire hyperoxalurie:bevinding:moment:bloed of weefsel:document:moleculair genetisch onderzoek
Synonyms: molgen
pl-PLPolish (Poland)Analiza wielogenowa pierwotnej hiperoksalurii:stwierdzenie:punkt w czasie:krew lub tkanka:dokument:genetyka molekularna
Synonyms: Analiza wielogenowa w kierunku PH diagnostyka molekularna
zh-CNChinese (China)原发性高草酸尿症多基因分析:发现:时间点:全血/组织:文档型:分子遗传学类实验室方法
Synonyms: 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 全血或组织;血液/组织;血液或组织 分子病理学;分子病理学试验 分子遗传学;分子遗传学方法;分子遗传学类方法;分子遗传学类检验方法;包括 RFL、PCR 及其他方法在内，用于在分子基础上检测遗传属性的方法的大类;聚合酶链反应;聚合酶链式反应 发现是一个原子型临床观察指标，并不是作为印象的概括陈述。体格检查、病史、系统检查及其他此类观察指标的属性均为发现。它们的标尺对于编码型发现可能是名义型，而对于叙述型文本之中所报告的发现，则可能是叙述型。;发现物;所见;结果;结论 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 血;血液

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CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=93843-1